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EP2451389B1 - Hüftgelenkvorrichtung - Google Patents

Hüftgelenkvorrichtung Download PDF

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Publication number
EP2451389B1
EP2451389B1 EP10797393.5A EP10797393A EP2451389B1 EP 2451389 B1 EP2451389 B1 EP 2451389B1 EP 10797393 A EP10797393 A EP 10797393A EP 2451389 B1 EP2451389 B1 EP 2451389B1
Authority
EP
European Patent Office
Prior art keywords
prosthetic
acetabulum
medical device
elongated
extending
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Active
Application number
EP10797393.5A
Other languages
English (en)
French (fr)
Other versions
EP2451389A1 (de
EP2451389A4 (de
Inventor
Peter Forsell
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Kirk Promotion Ltd
Original Assignee
Kirk Promotion Ltd
Kirk Promotion Ltd Oregon
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Kirk Promotion Ltd, Kirk Promotion Ltd Oregon filed Critical Kirk Promotion Ltd
Priority to EP15181461.3A priority Critical patent/EP3069691A1/de
Publication of EP2451389A1 publication Critical patent/EP2451389A1/de
Publication of EP2451389A4 publication Critical patent/EP2451389A4/de
Application granted granted Critical
Publication of EP2451389B1 publication Critical patent/EP2451389B1/de
Active legal-status Critical Current
Anticipated expiration legal-status Critical

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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2/32Joints for the hip
    • A61F2/36Femoral heads ; Femoral endoprostheses
    • A61F2/3609Femoral heads or necks; Connections of endoprosthetic heads or necks to endoprosthetic femoral shafts
    • AHUMAN NECESSITIES
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    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2/32Joints for the hip
    • A61F2/34Acetabular cups
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
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    • A61F2002/30001Additional features of subject-matter classified in A61F2/28, A61F2/30 and subgroups thereof
    • A61F2002/30108Shapes
    • A61F2002/3011Cross-sections or two-dimensional shapes
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    • A61F2002/30125Rounded shapes, e.g. with rounded corners elliptical or oval
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    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
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    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
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    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
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    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
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    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
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    • A61F2002/30001Additional features of subject-matter classified in A61F2/28, A61F2/30 and subgroups thereof
    • A61F2002/30316The prosthesis having different structural features at different locations within the same prosthesis; Connections between prosthetic parts; Special structural features of bone or joint prostheses not otherwise provided for
    • A61F2002/30329Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements
    • A61F2002/30331Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements made by longitudinally pushing a protrusion into a complementarily-shaped recess, e.g. held by friction fit
    • A61F2002/30354Cylindrically-shaped protrusion and recess, e.g. cylinder of circular basis
    • A61F2002/30355Cylinder of elliptical or oval basis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2002/30001Additional features of subject-matter classified in A61F2/28, A61F2/30 and subgroups thereof
    • A61F2002/30316The prosthesis having different structural features at different locations within the same prosthesis; Connections between prosthetic parts; Special structural features of bone or joint prostheses not otherwise provided for
    • A61F2002/30329Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements
    • A61F2002/30331Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements made by longitudinally pushing a protrusion into a complementarily-shaped recess, e.g. held by friction fit
    • A61F2002/30354Cylindrically-shaped protrusion and recess, e.g. cylinder of circular basis
    • A61F2002/30357Stepped cylinders, i.e. having discrete diameter changes
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2002/30001Additional features of subject-matter classified in A61F2/28, A61F2/30 and subgroups thereof
    • A61F2002/30316The prosthesis having different structural features at different locations within the same prosthesis; Connections between prosthetic parts; Special structural features of bone or joint prostheses not otherwise provided for
    • A61F2002/30329Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements
    • A61F2002/30331Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements made by longitudinally pushing a protrusion into a complementarily-shaped recess, e.g. held by friction fit
    • A61F2002/30362Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements made by longitudinally pushing a protrusion into a complementarily-shaped recess, e.g. held by friction fit with possibility of relative movement between the protrusion and the recess
    • A61F2002/30364Rotation about the common longitudinal axis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2002/30001Additional features of subject-matter classified in A61F2/28, A61F2/30 and subgroups thereof
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    • A61F2002/30329Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements
    • A61F2002/30331Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements made by longitudinally pushing a protrusion into a complementarily-shaped recess, e.g. held by friction fit
    • A61F2002/30362Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements made by longitudinally pushing a protrusion into a complementarily-shaped recess, e.g. held by friction fit with possibility of relative movement between the protrusion and the recess
    • A61F2002/30364Rotation about the common longitudinal axis
    • A61F2002/30365Rotation about the common longitudinal axis with additional means for limiting said rotation
    • AHUMAN NECESSITIES
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    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
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    • A61F2002/30329Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements
    • A61F2002/30469Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements using band clamps
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    • A61F2002/30471Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements connected by a hinged linkage mechanism, e.g. of the single-bar or multi-bar linkage type
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    • A61F2002/30535Special structural features of bone or joint prostheses not otherwise provided for
    • A61F2002/30604Special structural features of bone or joint prostheses not otherwise provided for modular
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    • A61F2/36Femoral heads ; Femoral endoprostheses
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    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2/46Special tools or methods for implanting or extracting artificial joints, accessories, bone grafts or substitutes, or particular adaptations therefor
    • A61F2002/4631Special tools or methods for implanting or extracting artificial joints, accessories, bone grafts or substitutes, or particular adaptations therefor the prosthesis being specially adapted for being cemented

Definitions

  • the present invention relates generally to medical devices for implantation in a hip joint
  • the hip joint is a synovial joint, joining the pelvis to the proximal portion of the femoral bone.
  • Synovial joints are the most common types of joints in mammals, and are typical of nearly all limb joints.
  • the contacting surfaces of said the pelvic, the acetabulum, and the contacting surface of the femoral bone, the caput femur, are smooth and rounded, and covered by articular cartilage.
  • a synovial membrane encapsulates the joint, forming a hip joint cavity, which contains synovial fluid. Outside the synovial membrane is a fibrous capsule and ligaments, forming an articular capsule.
  • Hip joint Osteoarthritis is a syndrome in which low-grade inflammation results in pain in the hip joints, caused by abnormal wearing of the Cartilage that acts as a cushion inside if the hip joint This abnormal wearing of the cartilage also results in a decrease of the joints lubricating fluid called Synovial fluid. Hip joint Osteoarthritis is estimated to affect 80% of all people over 65 years of age, in more or less serious forms.
  • the present treatment for hip osteoarthritis comprises NSAID drugs, local injections of Hyaluronic acid or Glucocorticoid to help lubricating the hip joint, and replacing parts of the hip joint with a prosthesis through hip joint surgery.
  • the replacing of parts of the hip joint is one of the most common surgeries to date performed at hundreds of thousands of patients in the world every year.
  • the most common method comprises placing a metal prosthesis in Femur and a plastic bowl in Acetabulum. This operation is done through an incision in the hip and upper thigh and through Fascia lata and the lateral muscles of the thigh. To get access to the joint, the supporting Capsule attached to Femur and Ilium needs to be penetrated, making it difficult to get a fully functional joint after the surgery.
  • Femur is then cut at the neck with a bone saw and the prosthesis is placed in femur either with bone cement or without.
  • Acetabulum is slightly enlarged using an Acetabular reamer, and the plastic bowl is positioned using screws or bone cement
  • the complications after hip joint surgery includes dislocation of the hip joint and loosening of the prosthesis from its fixation in the femoral bone.
  • the loosening and/or dislocation of the prosthesis could be induced by an abnormal strain being placed on the hip joint from e.g. the patient falling or making a rapid movement of the hip, or by a bodily macrophage reaction.
  • US patent application 2008/0228283 discloses an implant for use as a femur component having a femoral neck section comprising a femoral head axis and a contour in a cross-section perpendicular to the femoral neck axis tapering in a V-shape or wedge-shape.
  • German patent application DE 10 2004 008138 discloses a femoral prosthesis having a neck with an elliptical or rectangular cross-section.
  • a medical device for implantation in a hip joint of a patient is provided in accordance with claim 1.
  • Preferred embodiments are defined by the dependent claims.
  • the hip joint having a caput femur integrated with a collum femur having a collum and caput center axis, extending longitudinal along the collum and caput femur, in the center thereof
  • the medical device comprises: an elongated portion adapted to at least partially replace the collum femur, wherein said elongated portion is adapted to be connected to a prosthetic spherical portion adapted to replace the caput femur, and wherein said prosthetic spherical portion in turn is adapted to be movably placed in a prosthetic replacement for the acetabulum comprising at least one extending portion adapted to clasp said prosthetic spherical portion.
  • the elongated portion comprises a restricting portion adapted to restrict the motion range of the spherical portion in relation to the prosthetic replacement for the acetabulum.
  • the restricting portion of the elongated portion is adapted to enable an advantageous motion range in relation to the prosthetic replacement for the acetabulum
  • the hip joint is a synovial ball and socket joint which permits a large motion range for allowing a plurality of different movements of the lower limb. From a neutral position the following movements of the hip joint are normally possible: lateral or external rotation, 30° with the hip extended, 50° with the hip flexed, medial or internal rotation 40°, extension or retroversion 20°, flexion or anteversion 140°, abduction 50° with hip extended, 80° with hip flexed, adduction 30° with hip extended, 20° with hip flexed.
  • Centrally in the body should herein be understood as a pointof reference located at the intersection of the Median plane and the Coronal plane and in the center part of the heart along a longitudinal axis (Caudal - Cranial).
  • Proximal and distal are direction or location terms used in relation to said point centrally in the body and hence a distal point is a point farther away from the central point in relation a proximal point of the same structure.
  • Any plane disclosed herein is to be understood as having infinite extension.
  • Other anatomical terms used herein are further described in Moore et al., Clinically oriented anatomy,1999, Lippincott, Williams & Wilkins, Baltimore, pages 2 - 10 , which is hereby incorporated by reference.
  • Functional hip movements are to be understood as movements of the hip that at least partly correspond to the natural movements of the hip.
  • the natural movements of the hip joint might be some what limited or altered after hip joint surgery, which makes the functional hip movements of a hip joint with prosthetic surfaces somewhat different than the functional hip movements of a natural hip joint
  • Everyday activities is to be understood as activities which are not connected to any extreme movements, such that some physical sports require.
  • everyday activities comprise: walking, sitting, cycling etc.
  • the functional position of an implantable medical device or prosthesis is the position in which the hip joint can perform functional hip movements.
  • the final position is to be understood as a functional position in which the medical device needs no further position change to function.
  • Arthroscopy is to be understood as key hole surgery performed in a joint, since the arthroscopic procedure could be performed in the abdomen of the patient some of the steps of this arthroscopic procedure is more laparoscopic, however for the purpose of this invention the two terms arthroscopy and laparoscopy is used synonymously and for the purpose of this invention the main purpose of these methods are is that they are minimally invasive.
  • Elastic deformation is when a material deforms under stress (e.g. external forces), but returns to its original shape when the stress is removed.
  • a more elastic material is to be understood as a material having a lower modulus of elasticity.
  • the elastic modulus of an object is defined as the slope of its stress-strain curve in the elastic deformation region
  • the elastic modulus is calculated as stress / strain, where stress is the force causing the deformation, divided by the area to which the force is applied; and strain is the ratio of the change caused by the stress.
  • Elasticity is to be understood as a materials ability to deform in an elastic way.
  • Stiffness is to be understood as the resistance of an elastic body to deformation by an applied force.
  • Biocompatible material is to be understood as being a material with low level of immune response. Biocompatible materials are sometimes also referred to as biomaterials. Analogous is biocompatible metals a biocompatible metal with low immune response such as titanium or tantalum The biocompatible metal could also be a biocompatible alloy comprising at least one biocompatible metal.
  • Form fitting is to be understood as an element having a part or section which is adapted to enable a mechanical connection of said element to at least one other element using said part or section.
  • Form fitted structure is a structure of an element which enables form fitting.
  • Fig. 1a shows the pelvis in a frontal view.
  • Pelvis comprises the right and left hip bone making up the pelvic bone, in turn comprising the Sacrum 1803, Ilium 1802, Pubis 1804 and Ischium 1801.
  • the hip joint houses the right and left acetabulum 8a,b placed laterally and distally in the pelvis.
  • the acetabulum 8a,b being a spherically shaped cavity in the hip bones making up one of the parts of the hip joint, the acetabulum 8a,b being adapted to house the caput femur 5, being the proximal portion of the femoral bone 7 having a spherical contacting surface adapted to be placed in the acetabulum 8a,b and thus creating the operable hip joint
  • the pelvis has a right-left axis X extending substantially from the bottom of the left acetabulum 8a to the bottom of the right acetabulum 8b, the pelvis further having a caudal-cranial axis Y extending perpendicular to said right-left axis, centrally and substantially along the length of the patient, passing the dorsal portions of the pubic symphysis 1805 and substantially following the spinal cord 1806, intersecting the left-right axis X.
  • Fig. 1b shows the pelvis in a frontal view disclosing a second, displaced coordinate system.
  • the second displaced coordinate system has its origin O' in the bottom of the acetabulum bowl 8a.
  • the axis X and Y have, in a frontal view, been rotated the angle ⁇ , creating the axis X' and Y'.
  • the acetabulum center axis X' is aligned with the caput and collum femur center axis CX
  • the caput and collum femur center axis CX is an axis in the extension of the collum and caput femur axis, in the center thereof.
  • the hip joint substantially being in its base position when the patient is standing up or lying down.
  • the acetabulum center axis X' goes through a point O' being the origin O' in the bottom of the acetabulum bowl 8a, and a center point CP, being a point in the center of a circle defined by the edges of the acetabulum bowl 8a, and further trough the top of the caput femur 5 and following inside of the collum femur 6, aligned with the collum femur 6.
  • the axis Y' is perpendicular to the axis X and goes through the origin O' in the bottom of the acetabulum bowl 8a, parallel to a plane defined by the circle defined by the edges of the acetabulum bowl 8a.
  • Fig. 1c shows the right pelvic bone 9 in section disclosing the second, displaced coordinate system.
  • the origin O' is in the bottom of the acetabulum bowl 8.
  • the axis X' is aligned with the caput 5 and collum 6 femur center axis CX, when the hip joint is in its base position when the patient is standing up or lying down with extended leg.
  • the axis X' is goes through a point O' being the bottom of the acetabulum bowl 8, and a center point CP, being a point in the center of a circle defined by the edges of the acetabulum bowl 8, and further trough the top of the caput femur 5' and following inside of the collum femur 6, aligned with the collum femur 6.
  • the axis Y' is perpendicular to the axis X', goes through the origin O' in the bottom of the acetabulum bowl 8, parallel to the plane PC defined by the circle defined by the edges of the acetabulum bowl 8.
  • Fig.2a shows the pelvis in a lateral view, thus displaying the posterior side of Ilimu 1802, the anterior side of Ichum 1801, the anterior side of Pubis 1804, and Sacrum 1803 in a lateral view.
  • the pelvis has furthermore a dorsoventral axis Z being perpendicular to the caudal-cranial axis Y and the right-left axis Y shown in fig. 1 , and intersecting them both creating a common origin O for the three axis X,Y,Z.
  • the dorsoventral axis Z and the caudal-cranial axis Y thus being oriented such that a horizontal pelvis plane PXZ extends from the dorsoventral axis Z, and a coronal plane PXY extends from the dorsoventral axis Y.
  • Fig. 2b shows the pelvis in a plane view from the front and slightly from below, in the direction of the axis X' (further disclosed with reference to figs 1b and 1c ).
  • the view of fig 2b displaying the axis Y' and Z' with origin O' in the bottom of the acetabulum bowl 8 making up the acetabulum coordinate system
  • the axis Y', Z' in this plane view, dividing the acetabulum bowl 8 into four quadrants: the proximal-frontal quadrant 1807, the distal-frontal quadrant 1808, the distal-dorsal quadrant 1809 and the proximal-dorsal quadrant 1810.
  • Fig. 2c shows the pelvis in a perspective view from below and slightly from the front, displaying the right-left axis X passing through the center of the right and left acetabulum 8.
  • the right-left axis X is perpendicular to the dorsoventral axis Z which also is perpendicular to the caudal-cranial axis Y.
  • the coronal plane PXY extends from the dorsoventral axis Y, and the horizontal pelvis plane PXZ extends from the dorsoventral axis Z, thus being perpendicular to the coronal plane PXY.
  • Fig. 2d shows the coordinate system and planes of fig. 2c , it further shows the second, displaced, coordinate system, being the coordinate system of the acetabulum 8, also shown in fig. 2b .
  • the axis of the coordinate system of acetabulum X', Y', Z' having their origin O' in the bottom of the acetabulum bowl 8, the axis X being aligned with the caput and collum center axis.
  • FIG. 2d further discloses the vertical acetabulum plane PX'Y' and the horizontal acetabulum plane PX'Z', PX'Y' being defined by the axis X',Y' and the vertical acetabulum plane PX'Z' being defined by the axis X',Z'.
  • the planes PX'Y' and PX'Z' dividing the acetabulum bowl 8 into four quadrants, the proximal-frontal quadrant 1807, the distal-frontal quadrant 1808, the distal-dorsal quadrant 1809 and the proximal-dorsal quadrant 1810, in accordance with whatis previously disclosed, with reference to fig. 2b .
  • Fig. 2d further shows the location of foramen obturatum 1871.
  • Fig. 2e shows, schematically how the acetabulum coordinate system X,Y',Z' relates to the hemisphere defined by the acetabulum bowl 8.
  • Fig. 2f shows, schematically, how the vertical acetabulum plane PX'Y', and the horizontal acetabulum plane PX'Z' divides the acetabulum 8 into four quadrants; the proximal-frontal quadrant 1807, the distal-frontal quadrant 1808, the distal-dorsal quadrant 1809 and the proximal-dorsal quadrant 1810, in accordance with the previously disclosed, with reference to fig. 2b and 2d .
  • Fig 2g shows the view of fig. 2d , and in addition it shows the horizontal and vertical acetabulum planes PX'Y' and PX'Z' also being the caput and collum femur horizontal and vertical planes PX'Y' and PX'Z', analogically dividing the caput and collum femur into four quadrants.
  • Fig. 3a shows a perspective view of the hip joint in section, displaying the horizontal and vertical planes PX'Y' and PX'Z' originating from the caput 5 and collum 6 center axis CX and dividing the caput 5 and collum 6 femur into quadrants.
  • Fig. 3c shows the view of fig. 3b when a prosthetic acetabulum surface 65 has been placed in the acetabulum bowl 8 replacing the natural contacting surface of the acetabulum 8.
  • the prosthetic replacement for the acetabulum 8 comprises two extending portions 1823a,b adapted to clasp the spherical portion 45 being a prosthetic part adapted to replace the natural collum femur 5 and thus further restraining the prosthetic spherical replacement for the caput femur 45 in the prosthetic replacement for the acetabulum 65.
  • the prosthetic replacement for the acetabulum 65 and the prosthetic spherical replacement for the caput femur 45 combined creating a functional prosthetic hip joint Fig.
  • 3c further shows an elongated portion 2201, adapted to at least partially replace the collum femur.
  • the prosthetic spherical portion 45 and the elongated portion 2201 are connected to each other at the proximal portion of the elongated portion 2201.
  • the elongated portion 2201 is connected to a fixating portion 2202 adapted to be placed and fixated inside of the femoral bone 7.
  • the elongated portion 2201 restricts the movement of the spherical portion 45 in relation to the prosthetic replacement for the acetabulum 65, especially since the prosthetic replacement for the acetabulum comprises extending portions 1823a,b extending beyond the equator line of the prosthetic replacement for the acetabulum
  • the elongated portion thus further comprises a recess 2203 for enabling further movement of spherical portion 45 connected to the elongated portion 2201 in relation to the prosthetic replacement for the acetabulum 65.
  • Fig. 3d shows a perspective view of the hip joint in section, similar to the embodiment shown in fig. 3c .
  • the elongated portion 2201 comprises two recesses 2203a,b, placed such that the elongated portion 2201 are adapted to receive the extending portions 1823a,b through the extending portions 1823a,b entering the recesses 2203a,b of the elongated portion 2201 when the elongated 2201 and spherical 45 portions move in relation to the prosthetic replacement for the acetabulum 65.
  • Fig. 3e shows a perspective view of the hip joint in section, similar to the embodiment shown in fig. 3c and 3d .
  • the elongated portion 2201 is shaped such that the contacting portion between the elongated portion 2201 and the spherical portion 45 is eccentrically placed in relation to the center axis CX of the collum and caput femur.
  • the eccentrically placed contacting portion enables the spherical portion with the elongated portion to move more in one direction than in another.
  • This embodiment similar to the recess embodiments previously disclosed, enables the adaption of the elongated member to the prosthetic replacement for the acetabulum 65, and in particular the extending portions 1823a,b thereof, for enabling a particular motion pattern of the hip joint and thus the leg.
  • Fig. 4a shows a prosthetic spherical portion 45 and a prosthetic elongated portion 2201 in a schematic view, displaying the prosthetic elongated portion 2201 being connected to the prosthetic spherical portion 45.
  • the elongated portion 2201 does not have any recesses or adaptations facilitating the movement of the prosthetic portions in relation to a prosthetic replacement for the acetabulum comprising extending portions.
  • Fig. 4b shows a prosthetic spherical portion 45 and a prosthetic elongated portion 2201 in a schematic view in an embodiment where the elongated portion comprises a recess 2203a adapted to further enable movement of the prosthetic spherical 45 and elongated portions 2201 in relation to a prosthetic replacement for the acetabulum.
  • Fig. 4c shows a prosthetic spherical portion 45 and a prosthetic elongated portion 2201 in a schematic view in an embodiment in which the elongated portion 2201 comprises two recesses 2203a,b adapted to further enable movement of the prosthetic spherical 45 and elongated portions 2201 in relation to a prosthetic replacement for the acetabulum.
  • Fig. 4d shows a prosthetic spherical portion 45 and a prosthetic elongated portion 2201 in a schematic view in an embodiment in which the elongated portion 2201 is curved such that the area in which the elongated portion 2201 connects to the spherical portion 45 is eccentrically placed in relation to the collum and caput femur center axis CX.
  • Fig. 5 shows the prosthetic parts replacing the articulating surfaces of the hip joint
  • the prosthetic replacement for the acetabulum surface 65 comprises extending portions 1823a,b which are adapted to enter a recess 2203 of the prosthetic elongated portion 2201 adapted to at least partially replace the collum femur.
  • the recess enables further movement of the prosthetic spherical 45 and elongated 2201 portion in relation to the prosthetic replacement for the acetabulum 65 in the direction of recess, such as disclosed in the right part of fig. 5 , where the prosthetic part is placed in a state in which the prosthetic spherical 45 and elongated 2201 portions are moved maximally in the direction of the recess 2203.
  • Fig. 6a shows a cross-section of the prosthetic elongated portion without an adaptation to increase to motion range. This embodiment is disclosed in a schematic side view in fig. 4a .
  • Fig. 6b shows a cross-section of the prosthetic elongated portion having a recess 2203 or adaptation such that said elongated portion is adapted for further movement in relation to a prosthetic replacement for the acetabulum in the direction of the recess 2203 or adaptation.
  • This embodiment is disclosed in a schematic side view in fig. 4b .
  • Fig. 6c shows a cross-section of the prosthetic elongated portion where the restricting part of the elongated prosthetic portion is a narrow portion 2220, with a smaller cross-sectional area than other portions of the elongated portion.
  • the circular narrow portion 2220 disclosed in fig. 6c enables further movement of the prosthetic elongated portion in all radial directions. This embodiment is disclosed in a schematic side view in fig. 4c .
  • Fig. 6d shows a cross-section of the prosthetic elongated portion comprising two recesses 2203a and 2203b or adaptations, into which a prosthetic replacement for the acetabulum can enter for further increasing the motion range of the prosthetic hip joint in the directions of the recesses or adaptations.
  • This embodiment is disclosed in a schematic side view in fig. 4c .
  • Fig. 6e shows a cross-section of the prosthetic elongated portion wherein the restricting portion of the elongated portion has a narrow square cross-section such that for increasing the motion range of the prosthetic hip joint more in the directions of the sides of the square cross-section of the restricting portion of the elongated portion.
  • This embodiment is disclosed in a schematic side view in fig. 4c .
  • Fig. 6f shows a cross-section of the prosthetic elongated portion wherein the restricting portion of the elongated portion is more narrow that other portions of the elongated portions and eccentrically placed in relation to the caput and collum center axis.
  • the eccentric placement of the restricting portion of the elongated portion increases the motion range of the prosthetic hip joint in the direction of the recess created by the narrow portion being placed eccentrically.
  • Fig. 6g shows a cross-section of the prosthetic elongated portion similar to the embodiment shown in fig. 6f .
  • the narrow portion of the elongated portion is placed further eccentrically, further increasing the motion range of the prosthetic hip joint in the direction of the recess created by the narrow portion being placed eccentrically.
  • Fig. 6h shows a cross-section of the prosthetic elongated portion in which a potion of the elongated portion comprises a plurality of recesses 2203 which are adapted to a particular prosthetic replacement for the acetabulum.
  • the restricting portion is adapted for a prosthetic replacement for the acetabulum comprising extending portions with a circular surface entering the recess of the elongated prosthetic portion.
  • Fig. 6i shows a cross-section of the prosthetic elongated portion, wherein said cross section is a more narrow elliptically shaped cross section 2220 which enables further movement of the prosthetic elongated portion in the narrow direction of the elliptically shaped elongated portion.
  • Fig. 6j shows a cross-section of the prosthetic elongated portion in which a potion of the elongated portion comprises two recesses 2203a,b which are adapted to a particular prosthetic replacement for the acetabulum
  • the restricting portion is adapted for a prosthetic replacement for the acetabulum comprising extending portions with a circular surface entering the recess of the elongated prosthetic portion.
  • Fig. 6k shows a cross-section of the prosthetic elongated portion in an embodiment similar to the embodiment sown in fig. 6j , however, in the embodiment of fig. 6k the recesses 2203a,b are somewhat eccentrically placed in relation to the caput and collum center axis.
  • the eccentrically placed recesses 2203a,b thus altering the directions in which the motion range are further increased, such that the recesses could be adapted to more critical motions that a patient is interesting in doing.
  • Fig. 7a shows the prosthetic elongated portion 2201, also shown in fig. 6h , when placed in the prosthetic replacement for the acetabulum 65 in a cross-sectional view, and in a side view.
  • the prosthetic replacement for the acetabulum surface comprises four extending portions 1823a,b,c,d clasping the prosthetic spherical portion 45 when implanted in the functional position in the hip joint
  • Each of the extending portions 1823a,b,c,d of the prosthetic replacement for the acetabulum has a rounded shape adapted to match corresponding rounded recesses of the elongated portion 2201.
  • Fig. 7b shows the prosthetic elongated portion 2201, also shown in fig. 6i , when placed in the prosthetic replacement for the acetabulum 65 in a cross-sectional view, and in a side view.
  • fig. 7b shows the prosthetic elongated portion 2201, also shown in fig. 6i , when placed in the prosthetic replacement for the acetabulum 65 in a cross-sectional view, and in a side view.
  • the prosthetic replacement for the acetabulum surface comprises two rounded extending portions 1823c,d clasping the prosthetic spherical portion 45 when implanted in the functional position in the hip joint
  • the cross section of the prosthetic elongated portion is a more narrow, elliptically shaped cross section which enables further movement of the prosthetic elongated portion in the narrow direction of the elliptically shaped elongated portion, where according to this embodiment, the extending portions of the prosthetic acetabulum is placed.
  • Fig. 7c shows the prosthetic elongated portion 2201, also shown in fig. 6j , when placed in the prosthetic replacement for the acetabulum 65 in a cross-sectional view, and in a side view.
  • the prosthetic replacement for the acetabulum surface comprises two rounded extending portions 1823c,d clasping the prosthetic spherical portion 45 when implanted in the functional position in the hip joint
  • the two extending portions 1823c,d of the prosthetic replacement for the acetabulum has a rounded shape adapted to match corresponding rounded recesses of the elongated portion 2201.
  • the shape of the prosthetic replacement for the acetabulum 65 is so adapted that the prosthetic elongated portion 2201 can move along a relatively large motion range whilst the extending portions still clasping the prosthetic spherical portion 45.
  • Fig. 7d shows the prosthetic elongated portion 2201, also shown in fig. 6k , when placed in the prosthetic replacement for the acetabulum 65 in a cross-sectional view, and in a side view.
  • the prosthetic replacement for the acetabulum surface comprises two rounded extending portions 1823c,d , and one circumferentially elongated extending portion 1823b clasping the prosthetic spherical portion 45 when implanted in the functional position in the hip joint
  • the two extending portions 1823c,d of the prosthetic replacement for the acetabulum has a rounded shape adapted to match corresponding rounded recesses of the elongated portion 2201.
  • the third extending portion 1823b is not extending as far as the two 1823c and 1823d, thus not limiting the motion range as much.
  • the shape of the prosthetic replacement for the acetabulum 65 is so adapted that the prosthetic elongated portion 2201 can move along a relatively large motion range whilst the extending portions still clasping the prosthetic spherical portion 45.
  • Fig. 8a shows pelvis in the same view as fig. 2b .
  • the vertical and horizontal acetabulum planes PX'Y' and PX'Z' (further disclosed with reference to fig. 2d ) are shown in a strict plane view.
  • Two further planes PX"Y” is introduced in fig. 3 , which planes are rotated an angle ⁇ of 45° clockwise.
  • the planes PX"Y" and PX"Z in accordance with the planes PX'Y' and PX'Z' divides the acetabulum bowl into four different quadrants, being a proximal quadrant 1811, a frontal quadrant 1812, a distal quadrant 1813 and a dorsal quadrant 1814.
  • Fig. 8b shows a perspective view of the hip joint in section, displaying the horizontal and vertical planes PX'Y' and PX'Z' originating from the caput 5 and collum 6 center axis CX and dividing the caput 5 and collum 6 femur into quadrants.
  • Fig. 8b further shows the planes PX"Y" and PX"Z" dividing the acetabulum bowl into four different quadrants, being a proximal quadrant 1811, a frontal quadrant 1812, a distal quadrant 1813 and a dorsal quadrant 1814, which is further disclosed with reference to fig. 3a .
  • Fig. 9a shows a cross-section of an embodiment of the prosthetic elongated portion 2201, wherein said elongated portion is eccentrically placed in relation to the collum and caput center axis CX.
  • the eccentric placement of the elongated portion 2201 places a large portion of the elongated portion 2201a in the dorsal quadrant, smaller portions of the elongated portions 2201b,d in the proximal and distal quadrants, respectively, and a smaller portion 2201c is placed in the frontal quadrant
  • the placing of a larger portion of the restricting portion of the elongated portion 2201 in the dorsal quadrant 1814 limits the motion range in the extension mostly.
  • the movement range of the extension movements is less critical than for example flexion for every day activities, thus placing the major part of the elongated portion 2201a in the dorsal quadrant restricts the motion range needed in a less critical way.
  • the eccentrically placed elongated portion is further disclosed with reference to fig. 6f and 6g .
  • Fig. 9b shows a cross-section of an embodimentof the prosthetic elongated portion 2201, wherein said elongated portion comprises a recess 2203, mainly placed in the frontal 1812, proximal 1811 and distal 1813 quadrant, thus placing the major portion of the restricting portion of the elongated member in the dorsal quadrant 1814.
  • the placing of a larger portion of the restricting portion of the elongated portion 2201 in the dorsal quadrant 1814 limits the motion range in the extension mostly.
  • the movement range of the extension movements is less critical than for example flexion for every day activities, thus placing the major part of the elongated portion 2201a in the dorsal quadrant restricts the motion range needed in a less critical way.
  • the elongated portion comprising a recess is further disclosed with reference to fig. 4b and 6b .
  • Fig. 9c shows a cross-section of an embodiment of the prosthetic elongated portion 2201, wherein said elongated portion 2201 is curved such that the connecting area between the prosthetic spherical portion 45 and the prosthetic elongated portion 2201 is eccentrically placed in relation to the caput and collum center axis CX, thus placing the major portion of the restricting portion of the elongated member 2201 in the dorsal quadrant 1814.
  • the placing of a larger portion of the restricting portion of the elongated portion 2201 in the dorsal quadrant 1814 mainly limits the motion range in extension of the leg.
  • the movement range of the extension movements is less critical than for example flexion for every day activities, thus placing the major part of the elongated portion 2201a in the dorsal quadrant restricts the motion range needed in a less critical way.
  • the elongated portion comprising the curved elongated portion is further disclosed with reference to fig. 4d .
  • Fig. 10 shows a medical device for implantation in a hip joint of a patient
  • the medical device is adapted to be fixated to the pelvic bone of the patient, for example by means of an adhesive, such as bone cement, or mechanical fixating members, such as orthopedic screws.
  • the medical device comprises an inner 1827 and an outer 1828 surface. A contacting portion of the inner surface 1827 is spherical and faces the center of the hip joint, when the medical device is implanted.
  • the inside of the medical device is adapted to receive a caput femur or a prosthetic replacement therefor having a spherical portion, and the spherical contacting portion of the inner surface 1827 is adapted to be in contact with a spherical portion of the outer surface of the caput femur or a prosthetic replacement therefor.
  • the medical device according to the embodiment shown in fig. 4 comprises two extending portions 1823a,b, extending the contacting portion of the inner surface 1827' such that the extending portions 1823a,b clasps the spherical portion of caput femur or a prosthetic replacement therefor, for restraining the spherical portion in the medical device.
  • the medical device is adapted to receive the prosthetic spherical portion, connected to the prosthetic elongated portion.
  • the inner surface 1827 comprises an equator line 1821, being the largest circular circumference of the inner surface.
  • the two extending portions passes beyond the equator line 1821, such that an end portion 1829 of the contacting portion, here being of the extending portion 1823b of the inner surface 1827, forms a circular extension line 1822 placed distal to the equator line 1821, when the medical device is implanted, and having a smaller circumference than the equator line 1821; thus a distance 1826 between a center axis P of the medical device and the extension line 1822 is shorter than a distance 1825 between the center axis P and the equator line 1821.
  • Fig. 11 shows the medical device described with reference to fig. 10 when implanted.
  • the medical device is adapted to be fixated using orthopedic screws 1830, mechanically fixating the medical device to the pelvic bone 9, by the medical device comprising holes through which the screws 1830 are placed.
  • the contacting portion of the inner surface 1827 has been placed in contact with the prosthetic spherical portion being connected to a the prosthetic elongated portion 2201, the prosthetic spherical 45 and elongated portions 2201 replacing the proximal portion of the femoral bone.
  • the two extending portions 1823a and 1823b extending the contacting portion of the inner surface and clasping the spherical portion 45, for restraining the spherical portion in the medical device.
  • the inner surface comprising the equator line 1821, and the extending portions 1823a,b passing beyond the equator line 1821 and comprising the more distal extension line 1822 having a smaller circumference than the equator line 1821.
  • the more distal extension line 1822 being placed at a distance D1 from the equator line 1821.
  • the extension line 1822 is parallel to the equator line 1821, however this is not necessarily so in other embodiments.
  • the extension portion 1823a according to the embodiment shown in fig.
  • the recess 2203 in the elongated portion 2201 is adapted for some section of the extending portion to enter the recess 2203.
  • the extending portion could further be adapted to release the prosthetic spherical portion 45 when a large enough strain is placed on the joint This feature enables the prosthetic spherical portion to be fixedly attached in the prosthetic acetabulum 65 in normal use, and be released from the prosthetic acetabulum, e.g.
  • the extending elements are placed such that the extending elements restricts the motion range minimally, or in ways which are not limiting the motion range used in everyday life. This is enabled through the placing of the extending portions, or the interaction between the extending portion and adaptations of the prosthetic elongated portion.
  • the hip joint is a synovial ball and socket joint which permits a large motion range for allowing a plurality of different movements of the lower limb.
  • the following movements of the hip joint are normally possible: lateral or external rotation, 30° with the hip extended, 50° with the hip flexed, medial or internal rotation 40°, extension or retro version 20°, flexion or anteversion 140°, abduction 50° with hip extended, 80° with hip flexed, adduction 30° with hip extended, 20° with hip flexed.
  • abduction and adduction the depth of the acetabulumbowl and thus the extending portions does not restrict the motion range in a critical way since the motion range of the normal hip is restricted in these movements, in normally agile persons, by the muscles, tenors and ligaments sunrounding the hip joint
  • Fig. 12a shows a frontal view of pubis and the proximal portions of the femoral bones 7 when two embodiments prosthetic replacement for the acetabulum 65 has been implanted in the hip joint
  • the prosthetic replacements for the acetabulum shown comprises one extending portion 1823, here placed dorsal to the vertical acetabulum plane PX'Y', thus only partially limiting abduction in far excess of 50°.
  • the extending portion 1823 extends circumferentially along the equator line 1821 about 1/ 10 of the length of the equator line 1821, however in other embodiments the extending portion 1823 extends along as much as half of the length of the equator line 1821, and in other embodiments the extending portion 1823 extends as little as about 1/ 30 of the length of the equator line 1821.
  • the prosthetic replacement for the acetabulum placed in the left acetabulum 8b comprises two extending portions 1823a,b, both being placed dorsal the corresponding vertical acetabulum plane PX'Y' of the left acetabulum (not shown), thus limiting the motion range of the hip joint in a non restrictive way, in relation to everyday activities.
  • the extending portions 1823 extends discontinuously along the equator line 1821 thus enabling the elongated portion 2201 to partially be placed between the equator line and the extension line, and in the left embodiment, be placed between the extending portions 1823a,b thus entering the cavity between the extending portions 1823a,b.
  • the recess 2203 of the prosthetic elongated portion 2201 implanted in the right hip joint is radially placed, in relation to the caput and collum center axis, such that the a section of the prosthetic elongated portion 2201, can enter the recess for further increasing the movement range of the elongated 2201 and spherical 45a portion in relation to the prosthetic acetabulum surface 65.
  • the curving of the prosthetic elongated portion 2201 implanted in the left hip joint is radially placed, in relation to the caput and collum center axis, for further increasing the movement range of the elongated 2201 and spherical 45b portion in relation to the prosthetic acetabulum surface 65.
  • Fig. 12b shows a frontal view of pubis and the proximal portions of the femoral bones 7, when two further embodiments of the prosthetic replacements have been implanted.
  • the embodiment shown placed on the right side is an embodiment in which the prosthetic elongated portion 2201a adapted to replace the collum femur comprises a first 2203a and second 2203b recess placed at the restricting portion of the elongated portion 2201a.
  • the prosthetic elongated portion is connected to a prosthetic spherical portion 45a which is restrained in a prosthetic replacement for the acetabulum 65a fixated to the pelvic bone.
  • the prosthetic replacement for the acetabulum 65a comprises extending portions 1823 clasping the prosthetic spherical portion 45a and thus restraining the spherical portion if the prosthetic replacement for the acetabulum 65a.
  • the extending portions 1823 is placed in the proximal quadrants, thus limiting the motion range of the hip joint in a non restrictive way, in relation to everyday activities.
  • the extending portion 1823 extends circumferentially along the equator line 1821 about 1/ 10 of the length of the equator line 1821, however in other embodiments the extending portion 1823 extends along as much as half of the length of the equator line 1821, and in other embodiments the extending portion 1823 extends as little as about 1/ 30 of the length of the equator line 1821.
  • the prosthetic elongated portion 2201b shown placed in the left hip joint comprises a narrow portion connected to the prosthetic spherical portion 45b.
  • the narrow portion enables a relatively large motion range in relation to the prosthetic replacement for the acetabulum 65b, even though the prosthetic replacement for the acetabulum comprises extending portions 1823a,b extending beyond the equator line of the prosthetic spherical portion 45b, thus clasping the spherical portion and restraining it in a fixated position.
  • Fig. 13 shows the pelvis and the proximal portions of the femoral bones 7 including the embodiment of fig. 12a , with the difference that the natural caput femur and a portion of the natural collum femur has been replaced by a prosthetic spherical portion 45 and a prosthetic elongated portion 2201.
  • the prosthesis further comprises a prosthetic stem 1831 adapted to be placed inside and fixated to the femoral bone, either using bone cement or by the surface of the stem being adapted to facilitate the growth-in of bone, thus fixating the stem.
  • the prosthetic elongated portion 2201 is here coordinated with the extending portions 1823 of the prosthetic replacement for the acetabulum 65a,b for further improving the motion range of the hip joint, or not limiting the natural motion range of the hip joint
  • Fig. 14 shows the medical device according to an embodiment in which the medical device comprises two extending portions 1823a,b.
  • the medical device is placed on a prosthetic elongated portion 2201, to which a prosthetic spherical portion 45 is attached.
  • the prosthesis further comprises a stem 1831 which is adapted to be fixated inside of the femoral bone 7.
  • the prosthetic elongated member 2201 is here adapted to further improve the motion range of the hip joint, or not limiting the natural motion range of the hip joint, by the prosthetic elongated portion 2201 comprising a recess 2203 in which the extending portions 1823 can enter.
  • the prosthetic replacement for the acetabulum 65 comprises two extending portions 1823a,b, both extending circumferentially along the equator line (as disclosed in for example fig. 5 ) dorsal to the caudal-cranial axis Y and being adapted to clasp the caput femur or a prosthetic replacement therefor.
  • the extending portions 1823a,b extending dorsal to the caudal-cranial axis Y and thus reducing the limiting effect that the extending portions 1823a,b, have on the motion range of the hip joint According to the embodiment shown in fig.
  • the extending portion 1823a, placed proximally in the acetabulum extends circumferentially a distance of about 1 ⁇ 4 of the length of the equator line
  • the extending portion 1823b, placed distally in the acetabulum extends circumferentially a distance of about 1/ 10 of the length of the equator line, however it is equally conceivable that this relationship is the other way around, or that any of the extending portions circumferentially extends a distance of as much as half of the length of the equator line, thus extending the entire distance of the equator line being dorsal to the vertical acetabulum plane PX'Y', or that any of the extending portions 1823a,b extends a distance being as little as 1/ 30 of the distance of the equator line.
  • the first extending portion 1823a extends in distal-lateral direction from the acetabulum
  • the second extending portion 1823a extends in distal-lateral direction from the
  • Fig. 15b shows the pelvis in a lateral view
  • the prosthetic replacement for the acetabulum 65 comprises two extending portions 1823a,b, the two extending portions 1823a,b extends in the proximal quadrant 1811 and the distal quadrant 1813, respectively.
  • the extending portions 1823 can be adapted to reduce the effects that the extensions have on the motion range of the hip joint
  • Fig. 16 shows the pelvis in a lateral view
  • the prosthetic replacement for the acetabulum 65 shown comprises one extending portion 1823 extending and being adapted to clasp the caput femur, or a prosthetic replacement therefor.
  • the extending portion 1823 extends circumferentially along the equator line within the proximal quadrant 1811, which is further disclosed with reference to fig. 3 .
  • the extending portion 1823 extends in distal-lateral direction from the acetabulum.
  • Fig. 17 shows the pelvis in a lateral view
  • the prosthetic replacement for the acetabulum 65 shown comprises a continuously extending portion 1823 with two extending portions 1823a and 1823b extending further in relation to the average extension of the extending portion.
  • the entire extending portion is placed in the proximal, distal and dorsal quadrants and the extending portions 1823a,b extending further than the average extension of the extending portion 1823 extends in the proximal and distal quadrant
  • Fig. 18 shows the pelvis in a lateral view
  • the prosthetic replacement for the acetabulum 65 shown comprises four extending portions 1823a,b,c,d, wherein the first 1823a and second 1823b extending portions extends in the proximal and distal quadrant, respectively, thus the first extending portion 1823a extending in distal-lateral direction from the acetabulum, and the second extending portion 1823b extending medially towards foramen obturatum.
  • the fourth extending portion 1823d extends in the dorsal quadrant in accordance with the third extending portion 1823c do not extend as far as the first and second extending portions.
  • Fig. 19 shows an alternative embodiment of the prosthetic replacement for the acetabulum 65.
  • the prosthetic replacement for the acetabulum 65 comprises a first part 1841 adapted to be fixated to the pelvic bone of the patient
  • the first part comprises an inner contacting surface adapted to be in movable connection with an outer contacting surface of a second part 1842.
  • the second part 1842 is rotatably fixated to the first part 1841 by a rotatable connecting member 1843.
  • An outer contacting surface of a prosthetic spherical portion 45 is adapted to be placed in contact with the inner surface of the second part 1842 and be movable in multiple directions, thus replicating the natural ball and socketjointofthe hip.
  • the second part 1842 comprises two extending portions 1823a,b extending beyond the equator line 1845 of the second part 1842.
  • the extending portions 1823a,b extends longitudinally discontinuously along the equator line, thus creating an area between the extending portions, in which area a portion of the prosthetic collum femur can be placed, thus being placed partially between the equator line 1845 and the extension line 1846.
  • the construction shown in fig. 13 enables the second part 1842 to rotate if the prosthetic elongated portion 2201 engages the extending portions 1823a,b, which are sloped for this purpose.
  • the second part 1842 are always placed such that the prosthetic elongated portion 2201 can be placed partially between equator line 1845 and the extension line 1846, which creates an optimal range of movement whilst the second part clasps the prosthetic spherical portion 45, and thus restricting the spherical portion 45 in the second part 1842 of the prosthetic replacement for the acetabulum 65.
  • Fig. 20a shows the prosthetic replacement for the acetabulum 65 in a perspective view from below according to one embodiment.
  • the prosthetic replacement for the acetabulum 65 comprises two extending portions 1823a, b.
  • the prosthetic replacement for the acetabulum 65 is according to this embodiment adapted to be fixated to the pelvic bone by means of an adhesive which is adapted to be placed in connection with the adhesive recesses 1870 of the outer surface of the prosthetic replacement for the acetabulum 65.
  • Fig. 20b shows a prosthetic replacement for the acetabulum65 similar to the prosthetic replacement for the acetabulum 65 disclosed with reference to fig. 20a , but with the difference that it comprises three equally extending portions 1823a,b,c.
  • Fig. 20c shows a prosthetic replacement for the acetabulum65, similar to the prosthetic replacement for the acetabulum 65 disclosed with reference to fig. 20a , but with the difference that it comprises two equally extending portions 1823a,b and one less extending portion 1823c.
  • Fig. 20d shows a prosthetic replacement for the acetabulum65 similar to the prosthetic replacement for the acetabulum 65 disclosed with reference to fig. 20a , but with the difference that it comprises four equally extending portions 1823a,b,c,d.
  • Fig. 20e shows a prosthetic replacement for the acetabulum65 similar to the prosthetic replacement for the acetabulum 65 disclosed with reference to fig. 20a , but with the difference that the two extending portions are placed further from each other, and thus being adapted to be placed in the proximal and distal quadrant, when implanted.
  • Fig. 20f shows a prosthetic replacement for the acetabulum65 similar to the prosthetic replacement for the acetabulum 65 disclosed with reference to fig. 20a , but further comprising a less extending portion 1823c placed between the first and second extending portions 1823a,b.
  • the extending portions of the prosthetic replacement for the acetabulum 65 which have been described could be made from an elastic material, enabling the extending portions to pass onto the a prosthetic spherical portion, according to any of the embodiments herein.
  • Fig. 21a shows the prosthetic elongated portion 2201, also shown in fig. 7a , when placed in the prosthetic replacement for the acetabulum65 in a cross-sectional view, and in a side view.
  • the prosthetic replacement for the acetabulum surface comprises four extending portions 1823a,b,c,d clasping the prosthetic spherical portion 45 when implanted in the functional position in the hip joint
  • Each of the extending portions 1823a,b,c,d of the prosthetic replacement for the acetabulum has a rounded shape adapted to match corresponding rounded recesses of the elongated portion 2201.
  • the motion range of the prosthetic spherical portion 45 and the prosthetic elongated portion 2201 is further increased.
  • the elongated portion 2201 is placed centered in relation to the collum and caput center axis, such that the an equal portion of the elongated portion is placed in the proximal 1811, distal 1813, frontal 1812 and dorsal 1814 quadrants, respectively.
  • Fig. 21b shows the prosthetic elongated portion 2201, also shown in fig. 7b , when placed in the prosthetic replacement for the acetabulum 65 in a cross-sectional view, and in a side view.
  • fig. 21b shows the prosthetic elongated portion 2201, also shown in fig. 7b , when placed in the prosthetic replacement for the acetabulum 65 in a cross-sectional view, and in a side view.
  • the prosthetic replacement for the acetabulum surface comprises two rounded extending portions 1823c,d clasping the prosthetic spherical portion 45 when implanted in the functional position in the hip joint
  • the cross section of the prosthetic elongated portion is a more narrow, elliptically shaped cross section which enables further movement of the prosthetic elongated portion in the narrow direction of the elliptically shaped elongated portion, where according to this embodiment, the extending portions of the prosthetic acetabulum is placed.
  • the prosthetic replacement for the acetabulum 65 and the prosthetic elongated portion 2201 are oriented in relation to the acetabulum, such that the extending portions 1823c,d are placed in the proximal 1811 and distal 1813 quadrant, and the major parts of the elongated portion 2201 are placed in the frontal 1812 and dorsal 1814 quadrants, while only minor parts are placed in the proximal 1811 and distal 1813 quadrants.
  • This configuration enables the prosthetic replacement for the acetabulum 65 to have extending portions 1823c,d,, and the elongated portion to have a relatively large cross-section without restricting the motion range of the hip joint in excess of the restriction of a natural hip joint, in any direction.
  • Fig. 21c shows the prosthetic elongated portion 2201, also shown in fig. 7c , when placed in the prosthetic replacement for the acetabulum 65 in a cross-sectional view, and in a side view.
  • the prosthetic replacement for the acetabulum surface comprises two rounded extending portions 1823c,d clasping the prosthetic spherical portion 45 when implanted in the functional position in the hip joint
  • the two extending portions 1823c,d of the prosthetic replacement for the acetabulum 65 has a rounded shape adapted to match corresponding rounded recesses of the elongated portion 2201.
  • the shape of the prosthetic replacement for the acetabulum 65 is so adapted that the prosthetic elongated portion 2201 can move along a relatively large motion range whilst the extending portions still clasping the prosthetic spherical portion 45.
  • This configuration enables the prosthetic replacement for the acetabulum 65 to have extending portions 1823c,d, and the elongated portion to have a relatively large cross-section without restricting the motion range of the hip joint in excess of the restriction of a natural hip joint, in any direction.
  • Fig. 21d shows the prosthetic elongated portion 2201, also shown in fig. 7d , when placed in the prosthetic replacement for the acetabulum 65 in a cross-sectional view, and in a side view.
  • the prosthetic replacement for the acetabulum 65 comprises two rounded extending portions 1823c,d , and one circumferentially elongated extending portion 1823b clasping the prosthetic spherical portion 45 when implanted in the functional position in the hip joint
  • the two extending portions 1823c,d of the prosthetic replacement for the acetabulum 65 has a rounded shape adapted to match corresponding rounded recesses of the elongated portion 2201.
  • the third extending portion 1823b is not extending as far as the two 1823c and 1823d, thus not limiting the motion range as much.
  • the shape of the prosthetic replacement for the acetabulum 65 is so adapted that the prosthetic elongated portion 2201 can move along a relatively large motion range whilst the extending portions still clasping the prosthetic spherical portion 45.
  • the prosthetic replacement for the acetabulum 65 and the prosthetic elongated portion 2201 are oriented in relation to the acetabulum, such that the extending portions 1823c,d are placed in the proximal 1811 and distal 1813 quadrant, where only minor parts of the elongated portion 2201 are placed.
  • This configuration enables the prosthetic replacement for the acetabulum 65 to have extending portions 1823c,b,d in three directions, creating a very stable configuration, whilst still enabling the elongated portion to have a relatively large cross-section without restricting the motion range of the hip joint in far excess of the restriction of a natural hip joint
  • 1/ 10 of the cross section of the restricting portion of the elongated member is placed in the proximal and distal quadrants, whereas 9/ 10 are placed in the frontal and dorsal quadrants, which 9/ 10 could be equally distributed between the two quadrants, or a major part, such as 6/ 10 could be placed in the dorsal quadrant and 4/ 10 could be placed in the frontal quadrants, however it is equally conceivable that it is the other way around depending of the design of the prosthetic replacement for the acetabulum.
  • the medical device could comprise at least one material selected from a group consisting of: polytetrafluoroethylene (PTFE), perfluoroalkoxy (PFA) and fluorinated ethylene propylene (FEP).
  • PTFE polytetrafluoroethylene
  • PFA perfluoroalkoxy
  • FEP fluorinated ethylene propylene
  • the material comprises a metal alloy, such as cobalt-chromium-molybdenum or titanium or stainless steel, or polyethylene, such as cross-linked polyethylene or gas sterilized polyethylene.
  • ceramic material is also conceivable, in the contacting surfaces or the entire medical device such as zirconium or zirconium dioxide ceramics or alumina ceramics.
  • the part of the medical device in contact with human bone for fixation of the medical device to human bone could comprise a poorhouse structure which could be a porous micro or nano-structure adapted to promote the growth-in of human bone in the medical device for fixating the medical device.
  • the porous structure could be achieved by applying a hydroxy-apatite (HA) coating, or a rough open-pored titanium coating, which could be produced by air plasma spraying, a combination comprising a rough open-pored titanium coating and a HA top layer is also conceivable.
  • HA hydroxy-apatite
  • the contacting parts could be made of a self lubricated material such as a waxy polymer, such as PTFE, PFA, FEP, PE and UHMWPE, or a powder metallurgy material which could be infused with a lubricant, which preferably is a biocompatible lubricant such as a Hyaluronic acid derivate. It is also conceivable that the material of contacting parts or surfaces of the medical device herein is adapted to be constantly or intermittently lubricated.
  • a self lubricated material such as a waxy polymer, such as PTFE, PFA, FEP, PE and UHMWPE
  • a powder metallurgy material which could be infused with a lubricant, which preferably is a biocompatible lubricant such as a Hyaluronic acid derivate. It is also conceivable that the material of contacting parts or surfaces of the medical device herein is adapted to be constantly or intermittently lubricated.
  • the parts or portions of the medical device could comprise a combination of metal materials and/ or carbon fibers and/ or boron, a combination of metal and plastic materials, a combination of metal and carbon based material, a combination of carbon and plastic based material, a combination of flexible and stiff materials, a combination of elastic and less elastic materials, Corian or acrylic polymers.

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  • Health & Medical Sciences (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Cardiology (AREA)
  • Oral & Maxillofacial Surgery (AREA)
  • Transplantation (AREA)
  • Engineering & Computer Science (AREA)
  • Biomedical Technology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Vascular Medicine (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Prostheses (AREA)

Claims (12)

  1. Medizinische Vorrichtung zur Implantation in einem Hüftgelenk eines Patienten, wobei das Hüftgelenk einen Hüftkopf (5) mit integriertem Femurhals (6) mit einer Hals- und Kopf-Mittelachse (CX) aufweist, die sich in Längsrichtung entlang des Femurhalses und Hüftkopfes in der Mitte davon erstreckt, worin die medizinische Vorrichtung Folgendes umfasst:
    a) einen langgestreckten Abschnitt (2201), der ausgelegt ist, den Femurhals zumindest teilweise zu ersetzen, worin der langgestreckte Abschnitt ausgelegt ist, zumindest in einen kugelförmigen Prothesenabschnitt (45) als Ersatz des Hüftkopfes integriert oder damit verbunden zu sein, und worin der kugelförmige Prothesenabschnitt wiederum ausgelegt ist, beweglich in einem Prothesenersatz für die Hüftpfanne (65) platziert zu werden, der an dem Beckenknochen (9; 1801; 1802; 1803; 1804) fixiert wird und zumindest einen verlängerten Abschnitt (1823) zum Umklammern des kugelförmigen Prothesenabschnitts aufweist; worin:
    i) der langgestreckte Abschnitt einen Begrenzungsabschnitt umfasst, der ausgelegt ist, den Bewegungsbereich des kugelförmigen Abschnitts bezüglich des Prothesenersatzes für die Hüftpfanne einzuschränken,
    ii) der Begrenzungsabschnitt des langgestreckten Abschnitts ausgelegt ist, einen vorteilhaften Bewegungsbereich bezüglich des Prothesenersatzes für die Hüftpfanne zu ermöglichen, dadurch gekennzeichnet, dass
    b) ein Hauptabschnitt des Begrenzungsabschnitts des langgestreckten Abschnitts ausgelegt ist, nach Implantation und in einer definierten Grundstellung in dem dorsalen Quadranten (1814) platziert zu werden, so dass Streckung stärker eingeschränkt wird als Beugung.
  2. Medizinische Vorrichtung nach Anspruch 1, worin der erste Abstand ein Querschnittsabstand eines schmalen Abschnitts (2200) des langgestreckten Abschnitts ist, und worin der zweite Abstand ein Querschnittsabstand eines breiten Abschnitts des langgestreckten Elements ist.
  3. Medizinische Vorrichtung nach einem der Ansprüche 1 und 2, worin der langgestreckte Abschnitt zumindest eine Vertiefung (2203) aufweist, die ausgelegt ist, einen Abschnitt der künstlichen Hüftpfannenprothese nach der Implantation aufzunehmen.
  4. Medizinische Vorrichtung nach Anspruch 3, worin die Vertiefung ausgelegt ist, zumindest an einer der folgenden Stellen platziert zu werden:
    a) frontal zu der koronalen Beckenebene (PXY), nach Implantation und in einer definierten Grundstellung,
    b) in dem frontalen Quadranten (1812), nach Implantation und in einer definierten Grundstellung,
    c) in dem proximalen Quadranten (1811), nach Implantation und in einer definierten Grundstellung, und
    d) in dem distalen Quadranten (1813), nach Implantation und in einer definierten Grundstellung.
  5. Medizinische Vorrichtung nach einem der Ansprüche 3 und 4, worin die Vertiefung mehr als eines der Folgenden ist:
    a) 2 mm tief,
    b) 4 mm tief,
    c) 6 mm tief, und
    d) 8 mm tief.
  6. Medizinische Vorrichtung nach Anspruch 6, worin der Begrenzungsabschnitt einen gebogenen Abschnitt des langgestreckten Abschnitts umfasst, und worin der gebogene Abschnitt so gebogen ist, dass der Begrenzungsabschnitt des langgestreckten Abschnitts nach Implantation und in einer definierten Grundstellung hauptsächlich in dem dorsalen Quadranten (1814) platziert wird.
  7. Medizinische Vorrichtung nach Anspruch 1, worin der Begrenzungsabschnitt des langgestreckten Abschnitts ausgelegt ist, nach Implantation und in einer definierten Grundstellung im Wesentlichen mit der Hals-Mittelachse ausgerichtet zu werden, und ausgelegt ist, bezüglich der Halsachse exzentrisch platziert zu werden.
  8. Medizinische Vorrichtung nach einem der vorhergehenden Ansprüche, worin ein Querschnitt des Begrenzungsabschnitts des langgestreckten Abschnitts senkrecht zu der Hals-Mittelachse zumindest kreisförmig, polygonal oder elliptisch ist.
  9. Medizinisches Vorrichtungssystem, umfassend eine medizinische Vorrichtung nach einem der vorhergehenden Ansprüche, und einen Prothesenersatz für die Hüftpfanne, umfassend zumindest einen verlängerten Abschnitt zum Umklammern des kugelförmigen Abschnitts, worin der Prothesenersatz für die Hüftpfanne eine Innen- und eine Außenseite umfasst, worin ein Kontaktabschnitt der Innenseite kugelförmig und ausgelegt ist, zur Mitte des Hüftgelenks zu weisen, wen die medizinische Vorrichtung implantiert ist, und worin der Prothesenersatz für die Hüftpfanne ausgelegt ist, den kugelförmigen Abschnitt aufzunehmen, worin der Prothesenersatz für die Hüftpfanne zumindest einen verlängerten Abschnitt umfasst, der den Kontaktabschnitt der Innenseite so verlängert, dass der zumindest eine verlängerte Abschnitt den kugelförmigen Abschnitt umklammert, so dass der kugelförmige Abschnitt in der medizinischen Vorrichtung eingezwängt wird, und worin der Prothesenersatz für die Hüftpfanne ausgelegt ist, an dem Beckenknochen des Patienten fixiert zu werden.
  10. Medizinisches Vorrichtungssystem nach Anspruch 9, worin der Prothesenersatz für die Hüftpfanne ausgelegt ist, den kugelförmigen Abschnitt aufzunehmen, der mit der medizinischen Vorrichtung verbunden ist; worin:
    a) die Innenseite eine Äquatorlinie umfasst, die der größte Kreisumfang der inneren Kontaktfläche ist, die eine Fläche ist, die ausgelegt ist, mit dem kugelförmigen Abschnitt in Berührung zu sein, und
    b) der zumindest eine verlängerte Abschnitt (1823) die Äquatarlinie (1821) passiert, so dass der Endabschnitt des Kontaktabschnitts der Innenseite eine kreisförmige Verlängerungslinie mit einem kleineren Umfang als die Äquatorlinie formt, und
    c) sich der zumindest eine Verlängerungsabschnitt umfangsmäßig diskontinuierlich entlang der Äquatorlinie erstreckt, so dass ein Abschnitt der medizinischen Vorrichtung zwischen der Verlängerungslinie und der Äquatorlinie platziert werden kann.
  11. Medizinisches Vorrichtungssystem nach einem der Ansprüche 9-10, worin sich zwei Verlängerungsabschnitte umfangsmäßig entlang der Äquatorlinie erstrecken, zumindest in einem der Folgenden:
    a) dem distalen und proximalen Quadranten davon,
    b) dem proximalen und dorsalen Quadranten davon,
    c) dem distalen und dorsalen Quadranten davon,
    d) dem distalen, dorsalen und proximalen Quadranten davon, wenn der Prothesenersatz für die Hüftpfanne in seiner endgültigen Stellung platziert wird.
  12. Medizinisches Vorrichtungssystem nach einem der Ansprüche 9-11, worin der Verlängerungsabschnitt und der Begrenzungsabschnitt des langgestreckten Abschnitts ausgelegt sind, bei der Implantation in der Grundstellung im Verhältnis zueinander platziert zu werden, so dass zumindest eines der Folgenden zutrifft:
    a) Adduktion ist um mehr Grade eingeschränkt als Beugung,
    b) Abduktion ist um mehr Grade eingeschränkt als Beugung,
    c) Adduktion ist um mehr Grade eingeschränkt als Streckung, und
    d) Abduktion ist um mehr Grade eingeschränkt als Streckung.
EP10797393.5A 2009-07-10 2010-07-12 Hüftgelenkvorrichtung Active EP2451389B1 (de)

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US22978909P 2009-07-30 2009-07-30
US22976709P 2009-07-30 2009-07-30
US22975509P 2009-07-30 2009-07-30
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US10524918B2 (en) 2020-01-07
EP2451389A1 (de) 2012-05-16
WO2011005186A1 (en) 2011-01-13
ES2553392T3 (es) 2015-12-09
US20120109327A1 (en) 2012-05-03
EP2451389A4 (de) 2013-04-03
US20170312085A1 (en) 2017-11-02
US9649194B2 (en) 2017-05-16
US20200360146A1 (en) 2020-11-19

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